Biogenic volatile organic compound ambient mixing ratios and emission rates in the Alaskan Arctic tundra

H. Angot, Katelyn McErlean, Lu Hu, D. Millet, J. Hueber, Kaixin Cui, Jacob Moss, C. Wielgasz, Tyler Milligan, Damien T. Ketcherside, M. Bret-Harte, D. Helmig
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引用次数: 18

Abstract

Rapid Arctic warming, a lengthening growing season, and the increasing abundance of biogenic volatile-organic-compound-emitting shrubs are all anticipated to increase atmospheric biogenic volatile organic compounds (BVOCs) in the Arctic atmosphere, with implications for atmospheric oxidation processes and climate feedbacks. Quantifying these changes requires an accurate understanding of the underlying processes driving BVOC emissions in the Arctic. While boreal ecosystems have been widely studied, little attention has been paid to Arctic tundra environments. Here, we report terpenoid (isoprene, monoterpenes, and sesquiterpenes) ambient mixing ratios and emission rates from key dominant vegetation species at Toolik Field Station (TFS; 68°38′ N, 149°36′ W) in northern Alaska during two back-to-back field campaigns (summers of 2018 and 2019) covering the entire growing season. Isoprene ambient mixing ratios observed at TFS fell within the range of values reported in the Eurasian taiga (0–500 parts per trillion by volume – pptv), while monoterpene and sesquiterpene ambient mixing ratios were respectively close to and below the instrumental quantification limit (~ 2 pptv). Isoprene surface emission rates ranged from 0.2 to 2250 μgC m−2 h−1 (mean of 85 μgC m−2 h−1) and monoterpene emission rates remained, on average, below 1 μgC m−2 h−1 over the course of the study. We further quantified the temperature dependence of isoprene emissions from local vegetation, including Salix spp. (a known isoprene emitter), and compared the results to predictions from the Model of Emissions of Gases and Aerosols from Nature version 2.1 (MEGAN2.1). Our observations suggest a 180 %–215 % emission increase in response to a 3–4°C warming, and the MEGAN2.1 temperature algorithm exhibits a close fit with observations for enclosure temperatures in the 0–30°C range. The data presented here provide a baseline for investigating future changes in the BVOC emission potential of the under-studied Arctic tundra environment.
阿拉斯加北极冻土带生物源性挥发性有机化合物环境混合比和排放率
预计北极快速变暖、生长期延长以及生物源性挥发性有机化合物释放灌木丰度的增加都将增加北极大气中生物源性挥发性有机化合物(BVOCs),并对大气氧化过程和气候反馈产生影响。量化这些变化需要准确了解驱动北极BVOC排放的基本过程。虽然北方生态系统已被广泛研究,但对北极苔原环境的关注却很少。在这里,我们报告了Toolik野外站(TFS)主要优势植被物种的萜类(异戊二烯、单萜烯和倍半萜烯)环境混合比率和排放率;北纬68°38′,西经149°36′),在两次背对背的野外活动(2018年和2019年夏季)中覆盖整个生长季节。TFS观测到的异戊二烯环境混合率在欧亚针叶林报告的值范围内(0-500万亿分之一体积- pptv),而单萜和倍半萜环境混合率分别接近和低于仪器定量限值(~ 2 pptv)。异戊二烯表面发射率在0.2 ~ 2250 μgC m−2 h−1之间(平均为85 μgC m−2 h−1),单萜的发射率在整个研究过程中平均保持在1 μgC m−2 h−1以下。我们进一步量化了当地植被,包括Salix spp.(一种已知的异戊二烯排放者)的异戊二烯排放对温度的依赖性,并将结果与《自然》2.1版气体和气溶胶排放模型(MEGAN2.1)的预测结果进行了比较。我们的观测结果表明,当温度升高3-4°C时,排放量将增加180% - 215%,MEGAN2.1温度算法与0-30°C范围内的圈地温度观测结果非常吻合。本文提供的数据为研究北极冻土带环境中BVOC排放潜力的未来变化提供了基线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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